U.S. patent application number 13/060889 was filed with the patent office on 2012-02-02 for induction of p53 expression by neutralization of neuropilin-2 for the treatment of cancers.
Invention is credited to Christophe Borg, Camille Grandclement, John Wijdenes.
Application Number | 20120027779 13/060889 |
Document ID | / |
Family ID | 40481948 |
Filed Date | 2012-02-02 |
United States Patent
Application |
20120027779 |
Kind Code |
A1 |
Borg; Christophe ; et
al. |
February 2, 2012 |
Induction of p53 expression by neutralization of neuropilin-2 for
the treatment of cancers
Abstract
The present invention relates to the use of anti-human
neuropilin-2 antibodies, or of ligands of human neuropilin-2
derived from these antibodies, for obtaining a medicament intended
to increase p53 expression and to induce tumour cell apoptosis in
the context of an anticancer treatment.
Inventors: |
Borg; Christophe; (Pouillet
Les Vignes, FR) ; Wijdenes; John; (Larnod, FR)
; Grandclement; Camille; (Besancon, FR) |
Family ID: |
40481948 |
Appl. No.: |
13/060889 |
Filed: |
August 26, 2009 |
PCT Filed: |
August 26, 2009 |
PCT NO: |
PCT/FR09/01035 |
371 Date: |
October 18, 2011 |
Current U.S.
Class: |
424/174.1 ;
530/389.7 |
Current CPC
Class: |
A61K 2039/505 20130101;
A61P 35/00 20180101; C07K 16/2863 20130101; C07K 2317/56 20130101;
C07K 2317/73 20130101 |
Class at
Publication: |
424/174.1 ;
530/389.7 |
International
Class: |
A61K 39/395 20060101
A61K039/395; A61P 35/00 20060101 A61P035/00; C07K 16/30 20060101
C07K016/30 |
Foreign Application Data
Date |
Code |
Application Number |
Aug 27, 2008 |
FR |
084725 |
Claims
1. An Anti-human neuropilin-2 antibody, characterized in that the
binding thereof to tumour cells expressing human neuropilin-2
induces apoptosis of said tumour cells wherein the antibody is
chosen from the following: i. an antibody comprising the variable
domain of the heavy chain and the variable domain of the light
chain of the ITAC-B1 antibody, said domains being respectively
defined by the sequences SEQ ID NO: 2 and SEQ ID NO: 4; ii. an
antibody comprising the variable domain of the heavy chain and the
variable domain of the light chain of the ITAC-B2 antibody, said
domains being respectively defined by the sequences SEQ ID NO: 6
and SEQ ID NO: 8.
2. (canceled)
3. A polypeptide which binds to human neuropilin2, characterized in
that it comprises at least the CDR3 of the heavy chain and the CDR3
of the light chain of an antibody according to claim 1.
4. The polypeptide according to claim 3, characterized in that it
also comprises at least one CDR2 or CDR1 of the heavy chain and of
the light chain of the ITAC-B1 or ITAC-B2 antibody.
5-6. (canceled)
7. A method of treating a tumor containing tumor cells which
express human neuropilin-2 in a subject in of such treatment
comprising administering an amount of the antibody of claim 1
effective to bind to human neuropilin-2 on the tumor cell.
8. The method of claim 7 wherein the amount of amount of the
antibody is effective to increase p53 expression in the tumor cell
upon binding to human neuropilin-2.
9. The method of claim 7 wherein the amount of antibody is
effective to induce apoptosis of the tumor cell upon binding to
human neuropilin-2.
10. A method of treating a tumor containing tumor cells which
express human neuropilin-2 in a subject in of such treatment
comprising administering an amount of the polypeptide of claim 3
effective to bind to human neuropilin-2 on the tumor cell.
11. The method of claim 10 wherein the amount of amount of the
polypeptide is effective to increase p53 expression in the tumor
cell upon binding to human neuropilin-2.
12. The method of claim 10 wherein the amount of polypeptide is
effective to induce apoptosis of the tumor cell upon binding to
human neuropilin-2.
Description
[0001] The present invention relates to the treatment of cancer by
overexpression of the p53 tumour suppressor gene and induction of
tumour cell apoptosis by targeting of neuropilin-2.
[0002] Cancer is characterized by an uncontrolled cell
proliferation generally due to mutations in the genes that
upregulate (oncogenes) or downregulate (tumour suppressor genes)
cell proliferation. By virtue of their anarchical proliferation,
tumour cells locally invade healthy tissue and, after having
undergone further mutations, may acquire the ability to migrate in
the blood stream and to propagate remotely from the initial tumour
so as to form metastases. However, neovascularization of the tumour
by the angiogenesis mechanism is essential to tumour growth since
any cell, and in particular tumour cells which have a very high
oxygen and energy demand, cannot survive at more than a few ten
millimetres or so from a blood vessel.
[0003] The current anticancer treatments therefore have as their
main targets, on the one hand, the tumour cells themselves and, on
the other hand, the tumour angiogenesis.
[0004] As regards the anti-angiogenesis strategies, the involvement
of growth factors, in particular EGF or VEGF (Vascular Endothelial
Growth Factor), in the progression of cancers and in angiogenesis
has been demonstrated. Several molecules that target the action of
VEGFs have been developed as anti-angiogenesis medicaments: a
bevacizumab (Avastin.RTM.), which is to humanized monoclonal
antibody directed against VEGF, has been used since 2004 for the
treatment of metastatic colorectal cancer; sunitinib and sorafenib,
which are molecules that inhibit signal transduction in the
VEGF/VEGF-receptor pathway, have been used in anti-angiogenesis
strategies for the treatment of metastatic renal carcinoma.
[0005] As regards the strategies targeting the tumour and the
tumour cells, surgical ablation of tumour tissues (when this is
possible), solid-tumour radiotherapy, immunotherapies aiming at
strengthening the immune responses against the cancer cells, and
chemotherapies represent the standard therapeutic treatments. The
major advances in the understanding of the molecular mechanisms of
cancerogenesis have made it possible to develop new chemotherapies,
the effectiveness of which depends, however, on the type of cancer
to be treated and on the organ affected. In addition, many cancers
also pose major public health problems and prove to be resistant to
conventional therapies. For example, gastrointestinal cancers
(pancreatic cancer, cholangiocarcinomas, colorectal cancers)
rapidly become resistant to chemotherapy over the course of their
natural history. Loss of the tumour suppressor gene encoding the
p53 protein is one of the major mechanisms that explains the
resistance of tumour cells to apoptosis and to conventional
anti-neoplastic treatments such as chemotherapy or radiotherapy.
This is because the function of the p53 protein is to arrest the
cell cycle or to induce apoptosis of a cell in response to damage
to the cellular DNA or to oncogene activation. The p53 protein
therefore plays a central role in the control of the cell cycle and
in maintaining the integrity of the genome, by allowing the cell
whose cell cycle is interrupted to repair the genetic anomaly, or
else by bringing about its destruction through apoptosis. Since p53
is essential for protecting the organism against the effects of
aberrant or uncontrolled cell division, the absence of p53, its
underexpression or the expression of a nonfunctional p53 protein
results in the survival of tumour cells.
[0006] In an in vitro study model and in murine models, it has been
shown that restoring p53 expression by gene transfer promotes
cancer regression and improves the effectiveness of cytotoxic
treatments. In vitro studies have also shown that, in cells
expressing a wild-type protein and a mutant p53 protein having a
dominant negative effect with respect to the wild-type protein,
interference with an siRNA specifically targeting the mRNA encoding
the mutant p53 protein re-establishes the function of p53 (Martinez
et al. P.N.A.S., 99(23):14849-54, 2002). It has, moreover, been
shown that it is possible to "reactivate" mutant p53 proteins by
stabilizing a functional conformation of these proteins. The
CP-31398, PRIMA-1 and MIRA-1 molecules, the first molecules
developed that have this capacity, have been successfully used to
inhibit tumour growth in a model of human xenograft (for review,
cf. for example Levesque & Eastman, Carcinogenesis.,
28(1):13-20, 2007).
[0007] Restoration of the expression of a functional p53 protein,
and also induction of the overexpression of this protein, therefore
represent essential objectives in the development of antitumour
therapies.
[0008] The inventors have now demonstrated the existence of an
inverse correlation between neuropilin-2 (NRP-2) and expression of
the p53 protein, and have shown that, surprisingly, p53 expression
can be induced or increased by inhibiting neuropilin-2 expression
using siRNA.
[0009] Neuropilin-2, a transmembrane glycoprotein of approximately
130 kDa, is a receptor for semaphorins, in particular semaphorin
3F, and for growth factors of the VEGF family. It is expressed in
humans by neurons, endothelial cells and osteoblasts and by a wide
variety of neoplasms. It is composed of an intracytoplasmic domain
of approximately 40 amino acids, of a transmembrane domain and of
an extracellular domain. This extracellular domain comprises a
domain A, made up of 2 subdomains (a1a2), a domain B also made up
of 2 subdomains (b1b2), and a domain C. It has been shown that the
B domain constitutes the VEGF of binding site, whereas the binding
with semaphorin 3F involved both the A domain and the B domain
(Geretti et al., J. Biol. Chem., 282, 25698-707, 2007); the C
domain is, for its part, involved in the oligomerization of
NRP-2.
[0010] In many cases, the neuropilins are the only VEGF receptors
expressed by cancer cells (Bielenberg et al. Exp. Cell. Res.,
312(5):584-593, 2006), and several studies have shown that the
expression, or even the overexpression, of neuropilins is generally
correlated with an increase in tumour growth and in the invasive
and metastatic nature of cancers, and also with an unfavourable
prognosis.
[0011] In addition, many observations indicate that these receptors
play an essential role in tumour progression by activating
angiogenesis: in particular, the binding of VEGF to NRP-2 is
responsible for a pro-angiogenic activity, mediated by cooperation
between the short intracytoplasmic domain of NRP-2 and that of the
VEGF receptor VEGFR1. It has been reported that NRP-2 has the
ability to induce phosphorylation of the VEGFR1 receptor and of the
AKT protein, thus favouring the progression of cancers, and that
the suppression of neuropilin-2 with siRNA opposes the appearance
of metastases in xenografts and reduces tumour size (Gray et al. J.
Natl. Cancer Inst., 100:109-120, 2008). It has, moreover, been
shown that an anti-NRP-2 antibody (called anti-Nrp2.sup.B),
directed against the VEGF-binding site of the B domain of NRP-2,
can reduce tumour lymphangiogenesis and the formation of
metastases; this antibody acts by inhibiting lymphatic endothelial
cell migration, but has no effect on tumour cell migration,
proliferation or apoptosis (Caunt et al., Cancer Cell, 13, 331-42,
2008).
[0012] The inventors have generated anti-NRP-2 antibodies and have
noted that some of them produce the same effects on p53 expression
and the induction of apoptosis of tumour cells as the inhibition of
NRP-2 with siRNA, and that these effects are VEGF-independent. In
addition, they have noted in vitro and in vivo in a murine model
that these antibodies potentiate the effectiveness of anticancer
treatments.
[0013] These data open up new therapeutic perspectives, in
particular with regard to the possibility of developing innovative
strategies for sensitization to chemotherapy or to radiotherapy or
to other anticancer agents.
[0014] Thus, a subject of the present invention is an anti-human
neuropilin-2 antibody, or a ligand of human neuropilin-2 derived
from said antibody, characterized in that the binding thereof to
tumour cells expressing human neuropilin-2 induces apoptosis of
said tumour cells.
[0015] Advantageously, anti-human neuropilin-2 antibodies or
ligands in accordance with the invention, in addition to their
ability to induce apoptosis of tumour cells expressing human
neuropilin-2, have the following characteristics: [0016] they
induce p53 expression, and their ability to induce apoptosis is
dependent on this p53 expression (it is decreased by a p53
inhibitor, pifithrin-.alpha.); [0017] their neuropilin-binding
properties and their ability to induce apoptosis are
VEGF-independent (their binding to the surface of tumour cells
expressing human neuropilin-2 and their ability to induce apoptosis
of said cells are not modified by the presence of VEGF).
[0018] Antibodies in accordance with the invention may thus be
selected, from anti-human neuropilin-2 antibodies or from ligands
derived therefrom, on the basis of their ability to induce
apoptosis of tumour cells expressing human neuropilin-2, and/or on
the basis of one or more of the other characteristics mentioned
above.
[0019] The antibodies in accordance with the invention may be
natural polyclonal or monoclonal antibodies, or recombinant
antibodies, in particular chimeric or humanized antibodies. The
term "chimeric antibody" is intended to mean an antibody which has
the variable domains of the monoclonal antibody from which it is
derived, coupled to the constant domains of another antibody,
preferably a human antibody.
[0020] The term "humanized antibody" refers to an antibody
initially produced by a nonhuman animal, preferably the mouse,
having conserved its neuropilin-2-binding specificity, but in
which, in order to reduce its immunogenicity in humans, as many
murine sequences as possible have been replaced with the
corresponding human sequences. As regards the variable domains, the
sequences replaced are in general the FR (framework) regions, i.e.
the sequences located between the hypervariable loops, CDRs.
[0021] Chimeric or humanized antibodies in accordance with the
invention are preferably immunoglobulins of the IgG class, and in
particular of isotypes IgG1, 2, 3 or 4.
[0022] The expression "ligand of human neuropilin-2 derived from an
anti-neuropilin-2 antibody" is intended to mean any neuropilin-2
ligand comprising at least the CDR3s of the heavy chain and those
of the light chain of said antibody, and preferably also comprising
the CDR2s and/or the CDR1s of the heavy chain and of the light
chain of said antibody.
[0023] Neuropilin-2 ligands in accordance with the invention may in
particular be: [0024] any fragment of an anti-neuropilin-2 antibody
in accordance with the invention comprising at least the CDR3s, and
preferably also comprising the CDR2s and/or the CDR1s, of the heavy
and light chains of said antibody; [0025] any recombinant protein,
including a recombinant immunoglobulin molecule, comprising an
anti-neuropilin-2 antibody fragment in accordance with the
invention as defined above.
[0026] Anti-neuropilin-2 antibody fragments in accordance with the
invention are in particular Fv, dsFv, Fab, Fab'2 or scFv fragments.
The Fv fragments are constituted of the variable domains of the
heavy and light chains, VH and VL, of an antibody, combined with
one another via hydrophobic interactions. The dsFv fragment is
constituted of a VH:: VL dimer linked via a disulphide bridge. The
scFv fragments are constituted of the variable portions of the
heavy and light chains of an antibody, linked to one another by
means of a flexible linker (Clackson et al., Nature, 352: 624-628,
1991), thus forming a single-chain protein. The Fab fragments
result from the action of papain on an immunoglobulin molecule, and
each contain a light chain and the first half of a heavy chain,
connected to one another by a disulphide bridge. The F(ab')2
fragment can be obtained by treatment of an antibody with pepsin:
this fragment comprises two Fab fragments and a part of the hinge
region. The Fab' fragments can be obtained from the F(ab')2
fragments by cleavage of the disulphide bridge in the hinge
region.
[0027] These antigen-binding fragments may also be combined in
order to obtain plurivalent derivatives, such as "diabodies" or
"triabodies", resulting from the association of 2 or 3 of these
antigen-binding fragments.
[0028] Recombinant proteins comprising an anti-neuropilin-2
antibody fragment in accordance with the invention may in
particular be: [0029] proteins associating at least one
anti-neuropilin-2 antibody fragment in accordance with the
invention with at least one fragment of another antibody; by way of
examples, mention will be made of bispecific immunoglobulins,
conjugates of an Fv or Fab fragment of an anti-neuropilin-2
antibody with an Fv or Fab fragment of an antibody with a different
specificity, "bispecific diabodies" resulting from the association
of an scFv fragment of an anti-neuropilin-2 fragment with an Fv or
Fab fragment of an antibody with a different specificity; [0030]
proteins associating at least one anti-neuropilin-2 fragment in
accordance with the invention with a molecule for prolonging its
plasma half-life when it is administered in vivo, in particular
with a water-soluble polypeptide of molecular mass sufficient for
the molecular mass of the fusion polypeptide thus obtained to be
greater than the renal filtration threshold.
[0031] Chimeric or recombinant antibodies, scFv fragments and
derivatives thereof, etc., can be obtained by conventional genetic
engineering techniques, such as those described by Sambrook et al.
(Molecular Cloning, A Laboratory Manual, 2nd Ed., Cold Spring
Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989).
[0032] Polynucleotides encoding the variable regions of an
anti-neuropilin-2 antibody in accordance with the invention can be
obtained by cloning said regions from a library of cDNA of a
hybridoma producing said antibodies. They can also be prepared
completely or partially by nucleic acid synthesis, based on the
nucleotide sequences of said variable regions.
[0033] Various methods for obtaining humanized antibodies are also
well known in themselves (for review, cf., for example, Almagro
& Fransson, Frontiers in Bioscience, 13, 1619-1633, 2008).
[0034] Mention may be made of the methods based on CDR grafting,
which consists in transferring the CDRs of a nonhuman antibody into
the framework regions (FR) of an antibody of human origin (cf., for
example, Routledge et al., "Reshaping antibodies for therapy", in
Protein Engineering of Antibody Molecules for Prophylatic and
Therapeutic Applications in Man, 13-44, Academic Titles,
Nottingham, England, 1993, or Roguska et al., Protein Engineering,
9(10): 895-904, 1996). The CDR grafting is generally completed by
optimization of the framework regions, which consists in modifying
some residues of the framework regions in order to increase the
antigen-binding affinity of the humanized antibody. The use of
combinatorial libraries makes it possible to simplify this
optimization step (Rosok et al. J. Biol. Chem. 271: 22611-22618,
1996; Baca et al. J. Biol. Chem. 272: 10678-10684, 1997). Another
strategy for antibody humanization consists in conserving only the
CDR3s of the heavy and light chains of the antibody of origin, and
in selecting the rest of the sequence from naive libraries of human
V genes (Rader et al., Proc. Natl. Acad. Sci. U.S.A. 95: 8910-8915,
1998).
[0035] Two examples of anti-human neuropilin-2 monoclonal
antibodies in accordance with the invention are the antibodies
ITAC-B1 and ITAC-B2 described below. These monoclonal antibodies
have been selected by the inventors on the basis of their ability
to induce apoptosis of tumour cells expressing NRP-2.
[0036] The sequences of the heavy chain and of the light chain of
ITAC-B1 and of ITAC-B2 were determined. These sequences, and also
the deduced polypeptide sequences, are represented in Table 1 below
(for the light chain and the heavy chain of ITAC-B1) and in Table 2
below (for the light chain and the heavy chain of ITAC-B2). The
nucleotide sequences are also represented in the sequence listing
in the annex, respectively under the numbers SEQ ID No. 1, 3, 5 and
7, and the polypeptide sequences are also represented,
respectively, under the numbers SEQ ID No. 2, 4, 6 and 8.
[0037] The CNCM 1-4054 hybridoma, which produces the ITAC-B1
antibody, was furthermore deposited, according to the Treaty of
Budapest, on 30 Jul. 2008, with the Collection Nationale de Culture
de Microorganismes [French National Microorganism Culture
Collection] (Institut Pasteur, 25 rue du Docteur Roux, 75724 Paris
Cedex 15, France, under the number CNCM 1-4054.
TABLE-US-00001 TABLE 1 ITAC-B1 Heavy chain (V-D-J region)
Nucleotide gaagttaagctgcaggagtcaggggcagagcttgtgaagccaggggcctcagt
sequence caagttgtcctgcacagtttctggcttcaacattaaagacacctatatacact
gggtgatacagaggcctgaacagggcctggagtggcttggaaggattgatcct
gcgaatggtaatactaaatatgacccgaagttccagggcaaggccactataac
agcagacacatcctccaacacagcctacctgcagctcagcagcctgacctctg
aggacactgccgtctattactgtgctagatgggcggttgtaggtgactactgg
ggccaaggcaccactctcacagtctcctcag (SEQ ID No. 1) Peptide
EVKLQESGAELVKPGASVKLSCTVSGFNIKDTYIHWVIQRPEQGLEWLGRIDP sequence
ANGNTKYDPKFQGKATITADTSSNTAYLQLSSLTSEDTAVYYCARWAVVGDYW GQGTTLTVSS
(SEQ ID No. 2) Light chain (V-J region) Nucleotide
gatattgtgatcacccactctacaaattcctgcatgtatcagcaggagacagg sequence
gttaccataacctgcaaggccagtcagagtgtgagtgatgatgtggcttggta
ccaacagaagccagggcagtctcctaaactgctgatatactctgcatccaatc
gctacactggagtccctgatcgcttcactggcagtggatatgggacggatttc
actttcaccatcagcactgtgcagcctgaagacctggcagtttatttctgtca
gcaggattatagctctcccacgttcggttctgggaccaagctggagctgaaac (SEQ ID No.
3) Peptide YCDHPLYKFLHVSAGDRVTITCKASQSVSDDVAWYQQKPGQSPKLLIYSASNR
sequence YTGVPDRFTGSGYGTDFTFTISTVQPEDLAVYFCQQDYSSPTFGSGTKLELK (SEQ
ID No. 4)
TABLE-US-00002 TABLE 2 ITAC-B2 Heavy chain (V-D-J region)
Nucleotide gaggtgcagctggaggagtcagggggaggcttagtgaagcctggagggtccct
Sequence gaaactctcctgtgcagcctctggattcactttcagtgactattacatgtatt
gggttcgccagactccggaaaagaggctggagtgggtcgcaaccattagtgat
ggtggtagttacacctactatccagacagtattaagggccgattcaccatctc
cagggacaatgccaggaacaacctgtaccttcaaatgagcagtctgaagtctg
aggacacagccatgtattactgtgcaagaggtgggccctataggtcctggttt
gctttctggggccaagggactctggtcactgtctctgcag (SEQ ID No. 5) Peptide
EVQLEESGGGLVKPGGSLKLSCAASGFTFSDYYMYWVRQTPEKRLEWVATISD sequence
GGSYTYYPDSIKGRFTISRDNARNNLYLQMSSLKSEDTAMYYCARGGPYRSWF AFWGQGTLVTVSA
(SEQ ID No. 6) Light chain (V-J region) Nucleotide
gatattgtgatcacccagactccactctccctgcctgtcagtcttggagatca sequence
agcctccatctcttgcagatctagtcagagcattgtgtatagtaatggaaaca
cctatttagaatggtacctgcagaaaccaggccagtctccaaagctcctgatc
tacaaagtttccaaccgattttctggggtcccagacaggttcagtggcagtgg
atcagggacagatttcacactcaagatcagcagagtggaggctgaggatctgg
gagtttattactgctttcaaggttcacatgttcctccgacgttcggtggaggc
accaagctggaaatcaaac (SEQ ID No. 7) Peptide
DIVITQTPLSLPVSLGDQASISCRSSQSIVYSNGNTYLEWYLQKPGQSPKLLI sequence
YKVSNRFSGVPDRFSGSGSGTDFTLKISRVEAEDLGVYYCFQGSHVPPTFGGG TKLEIK (SEQ
ID No. 8)
[0038] The sequences encoding the CDRs of ITAC-B1 and ITAC-B2 have
also been determined, from the sequences of the heavy chains and of
the light chains above, using the IMGT/V-QUEST software (Giudicelli
et al., Nucleic Acids Research 32, W435-W440, 2004). The deduced
polypeptide sequences are represented below in Table 3 for the
ITAC-B1 antibody, and Table 4 for the ITAC-B2 antibody. They are
also represented in the sequence listing in annex under the numbers
SEQ ID No. 9 to 20.
TABLE-US-00003 TABLE 3 ITAC-B1 Sequence Heavy chain VH-CDR1
GFNIKDTY (SEQ ID No. 9) VH-CDR2 IDPANGNT (SEQ ID No. 10) VH-CDR3
ARWAVVGDY (SEQ ID No. 11) Light chain VL-CDR1 QSVSDD (SEQ ID No.
12) VL-CDR2 SAS (SEQ ID No. 13) VL-CDR3 QQDYSSPT (SEQ ID No.
14)
TABLE-US-00004 TABLE 4 ITAC-B2 Sequence Heavy chain VH-CDR1
GFTFSDYY (SEQ ID No. 15) VH-CDR2 ISDGGSYT (SEQ ID No. 16) VH-CDR3
ARGGPYRSWFAF (SEQ ID No. 17) Light chain VL-CDR1 QSIVYSNGNTY (SEQ
ID No. 18) VL-CDR2 KVS (SEQ ID No. 19) VL-CDR3 FQGSHVPPT (SEQ ID
No. 20)
[0039] The antibodies comprising the variable domains of ITAC-B1
(i.e. comprising a heavy chain of which the variable domain is
defined by the sequence SEQ ID No. 2 and a light chain of which the
variable domain is defined by the sequence SEQ ID No. 4) or the
variable domains of ITAC-B2 (i.e. comprising a heavy chain of which
the variable domain is defined by the sequence SEQ ID No. 6 and a
light chain of which the variable domain is defined by the sequence
SEQ ID No. 8), and also the antibodies or antibody-derived ligands,
as defined above, comprising at least the CDR3s of ITAC-B1 or of
ITAC-B2, constitute preferred embodiments of the subject of the
present invention.
[0040] A subject of the present invention is also any
polynucleotide encoding an antibody in accordance with the
invention or encoding a ligand of human neuropilin-2 derived from
said antibody, and also a recombinant vector, in particular an
expression vector, containing said nucleotide. A subject of the
present invention is also cells which produce antibodies or
antibody derivatives in accordance with the invention. They may in
particular be hybridomas, for example the CNCM 1-4054 hybridoma,
and host cells transformed with an expression vector in accordance
with the invention. Said host cell may be a prokaryotic or
eukaryotic cell. Among the eukaryotic cells that can be used,
mention may in particular be made of plant cells, yeast cells, such
as Saccharomyces, insect cells, such as the cells of Drosophila or
of Spodoptera, and mammalian cells such as HeLa, CHO, 3T3, C127,
BHK, COS, etc, cells.
[0041] The construction of the expression vectors in accordance
with the invention, and the transformation of the host cells, can
be carried out by means of conventional molecular biology
techniques.
[0042] A subject of the present invention is also an anti-human
neuropilin-2 antibody in accordance with the invention, or a ligand
of human neuropilin-2 derived from said antibody, for use as a
medicament, in particular as an antitumour medicament.
[0043] According to one preferred embodiment of the present
invention, said medicament is intended to induce apoptosis of
tumour cells expressing neuropilin-2, in particular by increasing
p53 expression in said tumour cells.
[0044] The invention is applicable to all types of tumours
expressing neuropilin-2, and in particular to colorectal cancers,
to breast cancers, to kidney cancer and to melanomas. The
expression of neuropilin-2 in a tumour can readily be detected, for
example using anti-human neuropilin-2 antibodies.
[0045] For the implementation of the present invention, the
anti-human neuropilin-2 antibody or the ligand of human
neuropilin-2 in accordance with the invention may be administered
intravenously, intraarterially or intraperitoneally.
[0046] Advantageously, it may be administered in combination with
another antitumour agent.
[0047] Antitumour agents that can be used in combination with an
anti-human neuropilin-2 antibody or a ligand of human neuropilin-2
in accordance with the invention are in particular chemotherapy
agents (such as alkylating agents, nucleotide analogues or
topoisomerase inhibitors), ionizing radiation or biotherapies (in
particular targeted therapeutic molecules neutralizing, for
example, VEGF, or the EGF receptor, tyrosine kinase inhibitors or
inhibitors of the mTor pathway).
[0048] The present invention will be understood more clearly from
the further description which follows, which refers to nonlimiting
examples illustrating the effect of the inhibition of NRP-2 with
siRNA on p53 expression, and tumour cell apoptosis, and the
preparation of anti-NRP-2 antibodies reproducing these effects.
EXAMPLE 1
Generation of Cell Lines Exhibiting Human Neuropilin-2 at their
Membrane Surface
[0049] Two cell lines were transfected in order to express NRP-2 at
their surface. A murine line, the P815 mastocytoma (Diaclone),
which is an experimental tumour widely used as a model in tumour
immunology, and which does not naturally express human NRP-2, and
also a human tumour line, developed from HT29 colorectal cancer
cells, not naturally expressing NRP-2 at its membrane surface, were
transfected with a human-NRP-2 expression vector. The expression
vector used, based on a plasmid pcDNA3.1 (Invitrogen) has been
described by Rossignol M et al, (Genomics. 2000 Dec. 1;
70(2):211-22).
[0050] The transfect p815 murine line was used to produce murine
monoclonal antibodies directed against the human NRP-2
glycoprotein, and the transfected human line was then used in
functional experiments for evaluating the advantage of the
anti-NRP-2 antibodies.
[0051] The transfection of the lines was carried out using an
Effecten.RTM. kit (Qiagen). The P815 mastocytes and the HT29 tumour
cells were cultured in 20 ml of DMEM medium until a concentration
of 200 000 cells/ml was reached. The cells were then washed once
with 20 ml of PBS and brought to a concentration of
2.times.10.sup.5 cells/ml in 4 ml of DMEM medium in a flask. The
cells were then transfected with 1 .mu.g of vector (plasmid vector
at 1 .mu.g/.mu.l in TBE buffer).
[0052] The transfected P815 and HT29 cells were left in small
flasks and incubated at 37.degree. C. under 5% CO.sub.2 in a
humidified atmosphere, for 48 h. At D3, the culture media were
replaced with a new medium containing 0.8 mg/ml of geneticin (G418,
Invitrogen, France), for selection of the transfected cells.
[0053] The efficiently transfected cells expressing NRP-2 at their
surface are called P815-NRP-2 and HT29-NRP-2. The efficiency of
transfection is evaluated at D7 by membrane labelling with a murine
anti-human NRP-2 IgG antibody (Clone C9, Santa Cruz Biotechnology)
and then reading by flow cytometry. The result of the flow
cytometry study is represented in FIG. 1.
[0054] Panels A and C (P815 and HT29ctrl) of FIG. 1 represent the
results obtained by flow cytometry with the control cells, while
panels B and D (P815-NRP-2 and HT29-NRP-2) represent the results
obtained with cells expressing NRP-2 at their membrane surface. The
distribution curves in black lines represent the results of the
labelling with a control antibody, the distribution curves in grey
lines represent the results of the labelling with the murine
anti-human NRP-2 IgG antibody.
[0055] For each of the panels of FIG. 1, the number of events
(number of cells) is indicated on the y-axis, the fluorescence
intensity (corresponding to the labelling of the cells with the
murine anti-human NRP-2 IgG antibody) is represented on the x-axis.
Panels A and C (P815 and HT29ctrl) of FIG. 1 show that the
distribution peaks representing the P815 and HT29ctrl cell
population (noninfected controls) in contact with the anti-human
NRP-2 antibody (grey line) or with a control IgG antibody (black
line) superimposed: this signifies that the P815 and HT29ctrl cells
(noninfected controls) are no more heavily labelled with the
anti-human NRP-2 antibody than with a control IgG antibody and that
they do not therefore express NRP-2. On the other hand, when the
P815 and HT29 cells transfected with a human-NRP-2 expression
vector (panels B and D, P815-NRP-2 and HT29-NRP-2, respectively)
are brought into contact with the anti-human NRP-2 antibody, there
is a clear shift in the cell-population distribution peak towards
the right (grey-line peak) relative to the labelling with the
control IgG antibody (black-line peak). These results attest to the
fact that the transfected cells clearly express NRP-2 at their
membrane surface.
EXAMPLE 2
Production and Characterization of Anti-Human NRP-2 Monoclonal
Antibodies
[0056] An immunization protocol derived from that described by
Matthew and Sandrock (J. Immunol. Methods, 100: 73-82, 1987) was
used. In each experiment, five female Balb/C mice (Charles River
Laboratories) were immunized with P815-NRP-2 transfected cells once
a week for 5 weeks.
[0057] Each immunization consists of the administration, in the
"foot-pad", of 1.times.10.sup.6 P815-NRP-2 cells in each back foot
of the mouse (i.e. 2.times.10.sup.6 P815-NRP-2 per mouse). The
cells used for the immunization of a mouse were diluted in 25 .mu.l
of 1.times.PBS and in 25 .mu.l of Ribi adjuvant (Immunochem
Research, USA). 50 .mu.l of cell mixture were then injected into
each mouse (25 .mu.l per back foot) several times during the
immunization protocol. Five days after the final injection, the
lymph nodes of the mice were removed and the lymphocytes were fused
with a myeloma line. The fusion was carried out in the following
way: the lymphocytes removed were fused with X63/AG 8653 murine
myeloma cells (the lymphocyte/myeloma cell ratio is 5:1), in the
presence of polyethylene glycol (Kearney et al, J. of Immunol, 123:
1548, 1978). The P3.times.63/AG8.653 murine myeloma originates from
the ATCC (ref CRL-1580).
[0058] The suspension of fused cells was washed once, and cultured
on a selective medium composed of 500 ml of RPMI 1640 (Sigma,
France), supplemented with 10% of heat-inactivated FCS (Abcys,
France), 4 mM of L-glutamine (Sigma, France), 100 mg/ml of
streptomycin, 100 IU/ml of penicillin (Sigma, France), 13.6
.mu.g/ml of hypoxanthine, 0.19 mg/ml of aminopterin and 3.88 IU/ml
of thymidine (50.times. solution, Sigma, France). This medium
allows neither the survival of the myeloma cells that have not
fused, since the latter are incapable of synthesizing inositol
monophosphate, nor the survival of the lymphocytes, which do not
have the ability to multiply indefinitely in vitro. On the other
hand, the hybridomas survive because they have, on the one hand,
the ability to metabolize the exogenous hypoxanthine (property of
lymphocytes) and, on the other hand, the ability to multiply
indefinitely ("immortality") of the X63/AG 8653 cells.
[0059] Ten days after the fusion, the supernatants from the
cultures in which hybridoma growth was observed were tested in
order to detect the production of anti-NRP-2 monoclonal antibodies.
For this purpose, the supernatants of each hybridoma culture well
were tested by flow cytometry on the cell lines expressing or not
expressing neuropilin-2.
[0060] The hybridomas producing antibodies recognizing the
P815-NRP-2 line were cloned using the limiting dilution method
(seeding density of 1 cell per culture well).
[0061] Several candidates specifically recognizing NRP-2 were
generated and selected for their ability to induce apoptosis of
tumour cells expressing neuropilin-2, including the clones ITAC-B1
and ITAC-B2. The ITAC-B1 clone was deposited, according to the
Treaty of Budapest, with the CNCM (Collection Nationale des
Microorganismes [French National Microorganism Collection],
Institut Pasteur, 25 rue du Docteur Roux, 75724 Paris Cedex 15,
France) on 30 Jul. 2008 under the deposit number CNCM 1-4054. In
order to characterize the ITAC-B1 and ITAC-B2 monoclonal
antibodies, membrane labelling was carried out by flow cytometry by
bringing 200 000 HT29, HT29-NRP-2, P815 or P815-NRP-2 cells into
contact with 5 .mu.g/ml of ITAC-B1 or of ITAC-B2, for 15 minutes at
4.degree. C. A goat anti-mouse secondary antibody coupled to FITC
was then incubated for 15 minutes in the dark, at 4.degree. C.,
before reading by flow cytometry. The results of the flow cytometry
analysis obtained for ITAC-B1 are represented in FIG. 2.
[0062] For each of the panels of FIG. 2, the number of events
(number of cells) is indicated on a y-axis, the fluorescence
intensity (corresponding to the labelling of the cells with the
ITAC-B1 antibody) is represented on the x-axis. Panels A and C
(P815+ITAC-B1 and HT29ctrl+ITAC-B1) of FIG. 2 represent the results
obtained by flow cytometry with the control cells, while panels B
and D (P815-NRP-2+ITAC-B1 and HT29-NRP-2+ITAC-B1) represent the
results obtained with cells expressing NRP-2 at their membrane
surface. The distribution curves in black lines represent the
results of the labelling with a control antibody, the distribution
curves in grey lines represent the results of the labelling with
the ITAC-B1 antibody. For cell lines expressing NRP-2, a clear
shift in the cell-population distribution peak towards the right is
noted when there is labelling with ITAC-B1 (grey line), in
comparison with the labelling with the control IgG antibody (black
line). For the cell lines not expressing NRP-2, this shift in the
distribution peak is very slight. These results show that the
ITAC-B1 antibodies specifically recognize the neuropilin-2 present
at the membrane surface.
[0063] Similar results were obtained for the ITAC-B2 antibody.
[0064] The genomic sequences of the variable region of the heavy
chains of the hybridomas producing the ITAC-B1 and ITAC-B2
antibodies were analysed by sequencing, respectively, with the
primers:
TABLE-US-00005 (degenerate sense primer) (SEQ ID No. 21)
5'-GARGTTAAGCTGSAGGAGTCAGG-3' (antisense primer) (SEQ ID No. 22)
5'-ATAGACAGATGGGGGTGTCGTTTTGGC-3'; and (sense primer) (SEQ ID No.
23) 5'-GAGGTGCAGCTGGAGGAGTCAGG-3' (antisense primer) (SEQ ID No.
24) 5'-ATAGACAGATGGGGGTGTCGTTTTGGC-3'.
[0065] The genomic sequences of the variable region of the heavy
chains of the hybridomas producing the ITAC-B1 and ITAC-B2
antibodies were analysed by sequencing, respectively, with the
primers:
TABLE-US-00006 (degenerate sense primer) (SEQ ID No. 25)
5'-GATATTGTGATSACMCARDCTACA-3' (antisense primer) (SEQ ID No. 26)
5'-GGATACAGTTGGTGCAGCATTA-3'; and (degenerate sense primer) (SEQ ID
No. 27) 5'-GATATTGTGMTSACCCAGACTCCA-3' (antisense primer) (SEQ ID
No. 28) 5'-GGATACAGTTGGTGCAGCATTA-3'.
[0066] The amino acid sequences of the CDR1, CDR2 and CDR3
hypervariable loops of the variable regions of the ITAC-B1 and
ITAC-B2 antibodies were determined using the IMGT/V-QUEST software,
version 3.0.0, on the immunoglobulin database of "the international
ImMunoGeneTics Information System.RTM." (IMGT/GENE-DB).
EXAMPLE 3
Role of Neuropilin-2 in Cell Proliferation
Production of a Vector Expressing Double-Stranded siRNAs Targeting
the Human NRP-2 Gene
[0067] A sense oligonucleotide: 5'-AAA GGC TGG AAG TCA GCA CTA
AT-3' (SEQ ID No. 29), and an antisense oligonucleotide: 5'-AAA AAT
TAG TGC TGA CTT CCA GC-3' (SEQ ID No. 30) corresponding to a part
of the gene sequence of human NRP-2, were hybridized, and the
resulting duplex was inserted into a dual-promoter expression
vector (pFiv H1/U6puro SiRNA Expression vector, System Biosciences)
digested beforehand with the BbsI enzyme.
[0068] After having verified that the insert indeed had the
expected size (21 base pairs), 100 .mu.l of competent E. coli HB101
bacteria (Gibco) were transformed with 1 .mu.g of the vector
containing this insert. A colony was amplified in 200 ml of LB
medium with ampicillin using a high-speed midi prep kit (Qiagen),
and then a maxiprep (Qiagen) was carried out and resulted in the
purification of the plasmid pFiv H1/U6puro SiRNA-NRP-2.
[0069] Since the plasmid pFiv H1/U6puro SiRNA-NRP-2 contains the H1
and U6 promoters of RNA polymerase III boarding the insert, each of
the strands of the insert is transcribed in the cells transfected
with this plasmid, resulting in the generation of double-stranded
siRNA directed against the NRP-2 transcripts, constituted of:
TABLE-US-00007 sense strand: (SEQ ID No. 31) 5'-GGC UGG AAG UCA GCA
CUA AUU U-3'; antisense strand: (SEQ ID No. 32) 5'-AUU AGU GCU GAC
UUC CAG CCU U-3'.
Production of a Cell Line Expressing an siRNA Targeting the Human
NRP-2 Gene
[0070] The Colo320 line naturally expressing neuropilin-2 at its
membrane surface was transfected with the plasmid pFiv H1/U6puro
siRNA-NRP-2 using the Effectene.RTM. kit, Qiagen). In parallel,
Colo320 cells were transfected with a control siRNA (siRNA-ctrl)
provided with the pFiv H1/U6puro SiRNA expression vector kit
(System Biosciences). The Colo320.sup.siRNA-NRP-2 and
Colo320.sup.siRNA-ctrl transfected cells were then selected at D2
with 2 .mu.g/ml of puromycin. The efficiency of the transfection
was evaluated from D7 onwards by labelling with a murine anti-human
NRP-2 IgG antibody (Clone C9, Santa Cruz Biotechnology) by flow
cytometry: the results obtained are represented in FIG. 3.
[0071] For each of the panels of FIG. 3, the number of events (the
number of cells) is indicated on the y-axis, the fluorescence
intensity (corresponding to the label of the cells with the
anti-NRP-2 antibody C9) is represented on the x-axis. The
distribution curves in black lines represent the results obtained
after labelling with a control antibody, the distribution curves in
grey lines represent the results obtained after labelling with the
C9 antibody. Panel B of FIG. 3, which represents the analysis
carried out with the Colo320.sup.siRNA-NRP-2 cells naturally
expressing NRP-2, shows a shift towards the left of the
distribution peak for the cells labelled with the C9 antibody,
compared with the analysis carried out with the
Colo320.sup.siRNA-ctrl cells, which is represented on panel A.
[0072] These results show that the expression of the NRP-2 protein
is efficiently inhibited in the cells expressing the
siRNA-NRP-2.
Assay for Proliferation in the Presence of siRNA-NRP-2: MTT
Test
[0073] The MTT proliferation assay is based on the reduction of
344,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide), by
the mitochondrial succinate dehydrogenase of active live cells, to
give formazan. The coloration intensity (OD) induced by this
reaction is proportional to the number of live cells present during
the assay, and to the metabolic activity thereof
[0074] 4000 HT29ctrl, HT29-NRP-2, Colo320.sup.siRNA-ctrl or
Colo320.sup.siRNA-NRP-2 cells were seeded into a 96-well Maxisorp
plate, in 100 .mu.l of DMEM medium containing 10% of inactivated
FCS. The assay was carried out in triplicate. At 24, 48 and 72
hours, respectively, 10 .mu.l of MTT at 5 mg/ml were added to each
well. After 2 hours of incubation at 37.degree. C., 5% CO.sub.2,
200 .mu.l of DMSO were added to each well after shaking, and the OD
was read at 570 nm using a spectrophotometer. The results of these
experiments are represented in FIG. 4.
[0075] FIGS. 4.A and 4.B are histograms representing the results
obtained in the proliferation assay carried out respectively with
the HT29ctrl and HT29-NRP-2 cells and with the
Colo320.sup.siRNA-ctrl and Colo320.sup.siRNA-NRP-2 cells. The
coloration intensity (the optical density "OD") corresponding to
the production of formazan by the cells is indicated on the y-axis,
and the times at which the viability tests were carried out are
indicated on the x-axis. For panel A, the light grey bars represent
the measurements carried out on the HT29-NRP-2 cells, and the dark
grey bars represent the measurements carried out on the HT29ctrl
control cells. For panel B, the light grey bars represent the
measurements carried out on the Colo320.sup.siRNA-NRP-2 cells, the
NRP-2 expression of which is suppressed, and the dark grey bars
represent the measurements carried out on the
Colo320.sup.siRNA-ctrl control cells expressing NRP-2.
[0076] FIG. 4.A shows that the OD increases when the cells express
NRP-2, which signifies that the expression of NRP-2 by the
HT29-NRP-2 cells induces cell proliferation and survival greater
than that of the cells not expressing NRP-2.
[0077] FIG. 4.B shows that the OD decreases when the NRP-2
expression in the Colo320 cells is suppressed (cf. bars
representing Colo320.sup.siRNA-NRP-2 in comparison with
Colo320.sup.siRNA-ctrl). This result confirms the result obtained
with the HT29 cells: NRP-2 induces a greater cell proliferation and
survival in the cells.
[0078] The influence of neuropilin-2 on the cell cycle was studied.
50 000 HT29 or HT29-NRP-2 cells were seeded, in 1 ml of DMEM-10%
FCS, in a 2-well plate. 24 hours after seeding, the cells were
trypsinized, washed twice with 3 ml of PBS and taken up in 1 ml of
70% ethanol. They were left at 4.degree. C., in 70% ethanol,
overnight. The following day, the cells were washed twice with 3 ml
of PBS, digested with Dnase and labelled with PI. 30 min later, the
cells were analysed using an EPIC'C Altra cytometer (Beckman
Coulter) and the Wincycles cycle analysis software. The results of
this analysis are given in FIG. 4bis.
[0079] FIG. 4bis shows that, when the cells express NRP-2, the
number of cells in G2M and S phase increases, whereas the number of
cells in G1 decreases. Thus, neuropilin-2 expression is associated
with an increase in the fraction of cells in S and G2M phase.
[0080] The oncogenic influence of neuropilin-2 was also evaluated
by comparing, in mice, the development of xenografts of various
tumour lines as a function of the expression of neuropilin-2 in
these lines.
[0081] FIGS. 5.A, 5.B, 5.0 and 5.D are photographs of mice having
been inoculated subcutaneously with the HT29ctrl, HT29-NRP-2,
Colo320.sup.siRNA-ctrl and Colo320.sup.siRNA-NRP-2 cells,
respectively.
[0082] While in mice inoculated with cells not expressing NRP-2
(FIG. 5.A and FIG. 5.D), there is no abnormal progression of the
xenograft, an abnormal increase in proliferation of the xenograft
is observed in the mice inoculated with cells expressing NRP-2
(FIG. 5.B and FIG. 5.C). These experiments show that the expression
of neuropilin-2 after transfection, or the repression of this
protein by interfering RNA, influences the oncogenesis of the
lines.
Modulation of p53 Expression with an siRNA Targeting the Human
NRP-2 Gene
[0083] The expression of p53, of E-cadherins and of cytokeratin 20
in xenografts of tumour cells expressing or not expressing
neuropilin-2 (HT29ctrl or HT29-NRP-2 line) was studied by
immunohistochemistry using antibodies specific for each of these
three proteins.
[0084] FIGS. 6.A, 6.0 and 6.E are photographs of sections of
xenografts taken in mice inoculated with the HT29ctrl control line,
and FIGS. 6.B, 6.D and 6.F are photographs of sections of
xenografts taken in mice inoculated with the line expressing NRP-2
(HT29-NRP-2).
[0085] The sections of xenografts of FIGS. 6.A and 6.B were
labelled with an anti-cytokeratin antibody, the sections of
xenografts of FIGS. 6.0 and 6.D were labelled with an
anti-E-cadherin antibody, and the sections of xenografts of FIGS.
6.E and 6.F were labelled with an anti-p53 antibody.
[0086] FIGS. 6.A, 6.C and 6.E show that the xenografts derived from
the HT29ctrl control line are strongly labelled with the
anti-cytokeratin, anti-E-cadherin and anti-p53 antibodies, whereas
the xenografts derived from the HT29-NRP-2 control line are not
labelled with any of these antibodies. This study showed that the
transfection of neuropilin-2, which promotes xenograft progression
(FIGS. 5.A to 5.D), is associated with a loss of expression of the
p53 anti-oncogene in the nuclei of the tumour cells (FIG. 6). In
addition, the immunohistochemical study shows a loss of E-cadherin
and cytokeratin 20 expression in the xenografts expressing
neuropilin-2 (FIG. 6), suggesting that the acquisition of
neuropilin-2 would promote epithelio-mesenchymal transition.
[0087] The influence of neuropilin-2 on p53 expression was also
studied. For this, the HT29-NP-2 or Colo320 lines were treated
either with siRNAs that inhibit the translation of neuropilin-2, or
with monoclonal antibodies originating from the ITAC-B1
hybridoma.
[0088] FIG. 7 represents the results obtained by flow cytometry for
the HT29-ctrl (panel A), HT29-NRP-2 (panel B),
Colo320.sup.siRNA-ctrl (panel C) and Colo320.sup.siRNA-NRP-2 (panel
D) cells labelled with an anti-p53 antibody. The curves in black
lines represent the results of the labelling with a control
antibody, and the curves in grey lines represent the results of the
labelling with the anti-p53 antibody. The number of events (the
number of cells) is indicated on the y-axis, the fluorescence
intensity (corresponding to the labelling of the cells with the
anti-p53 antibody) is represented on the x-axis.
[0089] Panels B and C showing the results obtained for the lines
expressing NRP-2, i.e. the panels HT29-NRP-2 and
Colo320.sup.siRNActrl, show that the p53 protein is not expressed
or is expressed very little (the curves of the populations labelled
with the control antibody or the anti-p53 antibody superimposed).
On the other hand, as regards panels A and D which show the results
obtained for the lines not expressing the NRP-2 protein, i.e. the
panels HT29ctrl and Colo320.sup.siRNA-NRP-2, when labelling is
carried out with the anti-p53 antibody (grey line), there is a
shift in the cell-population distribution peak towards the right,
in comparison with the labelling with control IgG antibody (black
line).
[0090] These experiments show that a negative correlation exists
between the presence of neuropilin-2 and that of p53. In
particular, when colo320, which is a tumour line constitutively
expressing neuropilin-2, is treated with interfering RNA so as to
inhibit the translation of this protein (Colo320.sup.siRNA-NRP-2
lines), restoration of p53 expression in the tumour lines is
clearly observed.
[0091] The protein extracts of the HT29-ctrl, HT29-NRP-2,
Colo320.sup.siRNA-ctrl and Colo320.sup.siRNA-NRP-2 lines were also
analysed by Western blotting using an anti-p53 antibody. After
lysis of the cell lines, migration of the protein pellets obtained
on a 10% polyacrylamide gel (10 .mu.g of protein per well,
standardized relative to the immunoblotting of actin), and then
transfer onto a PVDF membrane, the PVDF membrane was incubated
overnight with the p53 primary antibody (BD Biosciences, mouse
anti-human p53) diluted to 1/500. The membranes, after washing in
TBS/0.1% Tween20, were incubated for 1 hour with an anti-mouse HRP
secondary antibody diluted to 1/12 500. The results are represented
in FIG. 8.
[0092] FIG. 8 shows that the p53 protein is strongly expressed in
the HT29-ctrl line not expressing NRP-2, whereas it is undetectable
in the HT29-NP-2 line. Similarly, p53 cannot be demonstrated in the
Colo320.sup.siRNA-ctrl line which expresses NRP-2, whereas it is
strongly expressed in the Colo320.sup.siRNA-NRP-2 line in which the
expression of NRP-2 is repressed.
[0093] This experiment confirms that a negative correlation exists
between the presence of neuropilin-2 and the expression of p53.
[0094] These data indicate that the inhibition of neuropilin-2
expression makes it possible to increase p53 expression.
EXAMPLE 4
Effect of the ITAC-B1 antibody on tumour cell growth
[0095] Test for Formation of Tumour Colonies in a Semi-Solid Agar
Medium
[0096] In order to determine whether the ITAC-B1 antibody has a
neutralizing activity on the formation of tumour colonies in vitro,
tests for tumour colony formation in vitro in a semi-solid agar
medium containing agar were carried out. The principle of this test
is based on bringing Colo320 human tumour cells (which express
NRP-2 at their membrane surface and, furthermore, naturally secrete
VEGF into the culture medium) into contact with the ITAC-B1
antibody. 4000 Colo320 cells are seeded into each well of a 24-well
plate, in a semi-solid medium containing agar, and in the presence
of 10 .mu.g/ml of anti-NRP-2 antibody ITAC-B1. By way of
comparison, the same test is carried out in the presence of
cytotoxic agents with a proven action, i.e. 5-fluorouracil (5-FU),
used at a rate of 50 .mu.g/ml, or of Avastin.RTM. (bevacizumab:
humanized monoclonal antibodies directed against VEGF), used at a
rate of 50 .mu.g/ml, or in the presence of a control isotype
antibody (mouse IgG1 monoclonal antibody (BZ1)), used at a rate of
10 .mu.g/ml.
[0097] At 10 days post-seeding, the colonies were counted under an
optical microscope.
[0098] FIG. 9 represents the results obtained. The number of
colonies formed is indicated on the y-axis, and the various
molecules tested are indicated on the x-axis.
[0099] These results show that, in the presence of the ITAC-B1
antibody, as in the presence of 5-FU, the number of colonies is
approximately 40, versus more than 140 for the "cells alone"
control or the negative control, and approximately 120 colonies
when the cells are cultured in the presence of Avastin.RTM.
(bevacizumab).
[0100] It emerges from this in vitro study that the ITAC-B1
anti-NRP-2 antibodies almost completely inhibit the formation of
tumour colonies of cells expressing NRP-2 at their surface, in a
manner that is more efficient than with Avastin.RTM.
(bevacizumab).
[0101] Since neuropilin-2 is a coreceptor for VEGF, it was verified
whether the activity of ITAC-B1 was dependent on an interaction
between NRP-2 and the VEGF produced by the Colo320 cells. With this
aim, the tests for Colo320-cell colony formation were carried out
under the conditions described above, and in the presence of
ITAC-B1 antibody (10 .mu.g/ml), of bevacizumab (50 .mu.g/ml) or of
control antibody (10 .mu.g/ml), used separately or in
combination.
[0102] The results are given in FIG. 10: the y-axis represents the
number of colonies formed; on the x-axis, the antibodies present in
the culture medium are indicated by a "+".
[0103] FIG. 10 shows that the presence of bevacizumab in the
culture medium has very little effect on the proliferation of the
Colo320 cells: the number of colonies observed in the presence of
the control antibody, of bevacizumab, or of the combination of
these 2 antibodies is similar, and differs only slightly from that
observed with the "cells alone" control. On the other hand, the
number of colonies observed in the presence of the ITAC-B1 antibody
is greatly reduced compared with the "cells alone" control; in
addition, when the culture medium contains the ITAC-B1 antibody and
the bevacizumab (which neutralizes VEGF-A), the number of colonies
is identical to that observed when the medium contains the ITAC-B1
antibody alone. This result indicates that ITAC-B1 inhibits the
cell proliferation equally effectively in the presence of VEGF and
in the absence of VEGF, and therefore that the therapeutic effect
of ITAC-B1 is independent of the NRP-2/VEGF interaction.
MTT Assay for Tumour Cell Proliferation:
[0104] The effect of the ITAC-B1 antibody on the proliferation of
human tumour cells exhibiting NRP-2 at their membrane surface was
also studied using the MTT assay, as described in Example 3
above.
[0105] 4000 cells per well of Colo320.sup.siRNA-ctrl cells (control
cells transfected with an empty vector) or of
Colo320.sup.siRNA-NRP-2 cells (transfected with an siRNA targeting
NRP-2), in 100 .mu.l of DMEM medium containing 10% of inactivated
FCS, were seeded into a 96-well Maxisorp plate. After adhesion of
the cells, 5 .mu.g/ml of ITAC-B anti-NRP-2 antibody or 5 .mu.g/ml
of control antibody were added. After culture for 24, 48 or 72
hours, 10 p. 1 of MTT reconstituted at 5 mg/ml in PBS were added to
each culture well. The plates were then incubated for 3 hours in
the dark, at 37.degree. C. and 5% CO.sub.2, and centrifuged, and
then the supernatant was removed. 200 p. 1 of DMSO were then added
to each well. The optical density was read within an hour, at 570
nm, after shaking with the plate. The assay was carried out in
triplicate. The results are given in FIG. 11.
[0106] Panels A and B of FIG. 11 represent, respectively, the
results obtained in the proliferation assay carried out with the
Colo320.sup.siRNA-ctrl or Colo320.sup.siRNA-NRP-2 cells. The
optical density "OD" reflecting the production of formazan by the
cells is indicated on the y-axis, and the culture time is indicated
on the x-axis. The "cells alone" control is represented by
.diamond., the cells cultured in the presence of the control
antibody are represented by .box-solid., and the cells cultured in
the presence of the ITAC-B1 antibody are represented by
.DELTA..
[0107] These results shows that, in the case of the
Colo320.sup.siRNA-ctrl cells which express NRP-2, the proliferation
in the presence of the ITAC-B1 antibody is less than that of the
cells alone and that observed in the presence of the control
antibody. On the other hand, in the case of the
Colo320.sup.siRNA-NRP-2 cells, the proliferation in the presence of
the ITAC-B1 antibody is identical to that of the control cells and
to that observed in the presence of the control antibody. The
ITAC-B1 antibodies therefore specifically slow down the
proliferation of the cells exhibiting NRP-2 at the surface
(Colo320.sup.siRNA-ctrl cells) and not that of the cells not
expressing NRP-2 (Colo320.sup.siRNA-NRP-2 cells).
EXAMPLE 5
The ITAC-B1 Antibody has the Ability to Induce Apoptosis of Tumour
Cells Expressing Neuropilin-2
[0108] In order to determine the ability of the ITAC-B1 antibody to
induce apoptosis of tumour cells expressing NRP-2, an in vitro
Annexin V-APC apoptosis test was carried out (BD Pharmingen, San
Diego, Calif.). This test is based on the externalization of
phosphatidylserin by apoptotic cells and on the binding of Annexin
V-APC to this molecule.
1-Pro-Apoptotic Effect of ITAC-B1 Alone
[0109] 1 ml of DMEM medium containing 10% of inactivated FCS and
100 000 HT29-NRP-2 cells or 100 000 HT29ctrl cells were seeded, per
well, into a 24-well Nunc plate. After adhesion of the cells (3
hours), three concentrations of ITAC-B anti-NRP-2 antibody (0.5
.mu.g/ml, 1 .mu.g/ml and 5 .mu.g/ml) were tested in various wells.
In parallel, "cells alone" controls were carried out, as were
negative controls (anti-human mouse IgG1 antibody (BZ1) at the same
concentrations as the ITAC-B1 antibody).
[0110] After incubation for 16 hours, the culture supernatant was
drawn off and 500 .mu.l of trypsin-EDTA were added to each well and
left in contact for 10 minutes. When the cells began to detach, 500
.mu.l of DMEM medium-10% FCS were added per well. The cells were
then centrifuged, washed twice in PBS, and then taken up in 300
.mu.l of 1.times. binding buffer (provided in the kit), and then 5
.mu.l of Annexin V-APC were subsequently added to 100 .mu.l of this
solution. The flow cytometry analysis of the populations of cells
labelled with the Annexin V-APC as a function of the concentrations
of ITAC-B1 antibody, and of control antibody, is given in FIG.
12.
[0111] For each of the panels of FIG. 12, the number of events
(number of cells) is indicated on the y-axis and the fluorescence
intensity (corresponding to the labelling of the cells with the
Annexin V-APC) is represented on the x-axis. Panels A, C and E
represent the experiments carried out with the HT29-NRP-2 cells,
panels B, D and F represent the experiments carried out with the
HT29ctrl cells. The experiments for which the concentration of
ITAC-B1 antibody is 0.5 .mu.g/ml are represented in panels A and B
of FIG. 12. The experiments for which the concentration of ITAC-B1
antibody is 1 .mu.g/ml are represented in panels C and D of FIG.
12, and the experiments for which the concentration of ITAC-B1
antibody is 5 .mu.g/ml are represented in panels E and F of FIG.
12. For each panel, the distribution curve (1) represents the cells
alone, the distribution curve (2) represents the cells cultured in
the presence of a control murine isotype antibody and the
distribution curve (3) represents the cells cultured in the
presence of the ITAC-B1 antibody.
[0112] For panels C and E representing the experiments carried out
with the HT29-NRP-2 cells expressing NRP-2, a shift towards the
right is observed for the distribution peak corresponding,
respectively, to the concentrations of 1 and 5 .mu.g/ml of ITAC-B1
antibody. This shift in the distribution peak is not observed for
the "cells alone" and "control antibody" controls. This result
indicates that apoptosis is specifically induced in the cells
expressing NRP-2 starting from 1 .mu.g/ml of ITAC-B1 antibody in
the culture medium.
[0113] As regards the corresponding experiments carried out with
the HT29ctrl cells which do not express NRP-2, curves representing
the conditions: cells alone, and control-antibody and
ITAC-B1-antibody controls, are superimposed, indicating that the
ITAC-B1 antibody does not bring about the apoptosis of cells not
expressing NRP-2.
[0114] It is noted that the ITAC-B1 antibody induces apoptosis of
cells expressing NRP-2 at their cell surface, at a dose greater
than or equal to 1 .mu.g/ml. The apoptosis induced by ITAC-B1 is
dose-dependent since a higher concentration of ITAC-B1 leads to
greater apoptosis.
[0115] These experiments therefore show that the ITAC-B1 antibody
specifically induces apoptosis of tumour cells exhibiting NRP-2
(HT29-NRP-2) at their membrane surface, without inducing apoptosis
of cells not exhibiting NRP-2 (HT29).
II--Pro-Apoptotic Effect of ITAC-B1 in Combination with Other
Anticancer Agents
[0116] Similar experiments for evaluating the ability of ITAC-B1 to
induce apoptosis of cells expressing NRP-2 were carried out with
cells culturing the presence either of 5-FU (5-fluorouracil) or of
irinotecan, two anticancer agents commonly used in chemotherapy. In
this series of experiments, the ITAC-B1-antibody concentrations of
2.5 .mu.g/ml and 5 .mu.g/ml were tested. In parallel, "cells alone"
controls were carried out, as were controls with the BZ1 antibody
at the concentrations of 2.5 .mu.g/ml and 5 .mu.g/ml. The 5-FU and
the irinotecan were used at 10 .mu.g/ml. The results of these
experiments are represented in FIG. 13.
[0117] The panels of FIG. 13 are point-cloud representations of the
flow cytometry analysis. For each of the panels, the fluorescence
intensity (corresponding to the labelling of the cells with Annexin
V-APC) is represented on the x-axis. The y-axis indicates the
granulosity of the cells (Side Scatter or SSC). The
antibody-treatment conditions are indicated above the panels, and
the treatment with 5-FU or irinotecan is indicated to the right of
the panels. The percentage of cells labelled with Annexin V-APC
(corresponding to the percentage of cells having entered into
apoptosis) is indicated at the bottom-right of each panel.
[0118] The cells alone exhibit approximately 12% apoptosis, and the
cells cultured in the presence of 5-FU or irinotecan alone, or
combined with the BZ1 control antibody, exhibit between
approximately 34% and 43% apoptosis in the case of 5-FU, and
between 21% and 35% apoptosis in the case of irinotecan.
[0119] The apoptosis in the cells cultured jointly in the presence
of 5-FU and of the ITAC-B1 antibody is of the order of 78.5% for an
ITAC-B1 concentration in the medium of 2.5 .mu.g/ml, and of the
order of 80% for an ITAC-B1 concentration of 5 .mu.g/ml.
[0120] For the cells cultured in the presence of irinotecan and of
ITAC-B1, the apoptosis is of the order of 51% for an ITAC-B1
antibody concentration of 2.5 .mu.g/ml, and of the order of 58% for
a concentration of 5 .mu.g/ml.
[0121] These results therefore demonstrate a synergy of action
between the ITAC-B1 antibodies and the anticancer molecules, the
5-FU/ITAC-B1 combination being the most effective under the
conditions tested.
III--The Pro-Apoptotic Effect of ITAC-B1 is Correlated with p53
Expression
[0122] In order to correlate the induction of apoptosis with p53
expression, the Colo320siRNA-ctrl cells were pretreated for 18 h
with a chemical inhibitor of p53, pifithrin-.alpha., at a dose of
27 .mu.M (PFT.alpha., Sigma). After pretreatment, the cells are
washed twice with 3 ml of PBS and placed in a 24-well plate, at a
rate of 100 000 cells/well in 1 ml of RPMI-10% FCS. Non-pretreated
cells are placed under the same conditions. The cells are incubated
for 5 h with a control murine isotype antibody (BZ1) or ITAC-B1 at
20 .mu.g/ml and the apoptosis is measured as described above.
[0123] FIG. 14 represents the results of the apoptosis-induction
experiments carried out with the Colo320siRNA-ctrl cells pretreated
or not pretreated with PFT.alpha.. The percentage of cells labelled
with Annexin V-APC is indicated on the y-axis, the cell culture
conditions are indicated on the x-axis (control consisting of
medium, control consisting of medium supplemented with a control
isotype antibody -BZ1-, test consisting of medium supplemented with
the ITAC-B1 antibody). The results of the tests carried out with
cells pretreated with PFT.alpha. are represented in light grey,
those of the tests carried out with non-pretreated cells are
represented in dark grey.
[0124] While, in the control consisting of medium and the control
consisting of medium supplemented with control antibody the
labelling with Annexin V-APC is similar whether or not the cells
are treated with PFT.alpha., it is noted that the cells cultured in
the presence of ITAC-B1 antibody are more weakly labelled when they
are pretreated with PFT.alpha. (approximately 28% labelling versus
41% for the non-pretreated cells).
[0125] These results show that the pretreatment with PFT.alpha.
prevents the ITAC-B1-dependent apoptosis. The ITAC-B1-induced
apoptosis therefore appears to be dependent on p53 expression.
IV--The Pro-Apoptotic Effect of ITAC-B1 is VEGF-Independent
[0126] In order to determine whether the apoptotic effect observed
during the treatment of the cells with the ITAC-B1 antibody was
dependant on the binding of VEGF to NRP-2, the HT29-NRP-2 cells
expressing NRP-2 (and which, like the Colo320 cells, naturally
secrete VEGF into the culture medium) were cultured in the presence
of the anti-VEGF humanized monoclonal antibody Avastin.RTM.
(bevacizumab) at 50 .mu.g/ml, and the cells were then incubated in
the presence of a control murine isotype antibody (BZ1) or of
ITAC-B1 at 20 .mu.g/ml for 6 hours. The apoptosis induced was then
measured by labelling with Annexin V-APC as described above. The
results are given in FIG. 15.
[0127] The panels of FIG. 15 are point-cloud representations of the
flow cytometry analysis. For each of the panels, the fluorescence
intensity (corresponding to the labelling of the cells with Annexin
V-APC) is represented on the x-axis. The y-axis indicates the
granulosity (side scatter) of the cells. The conditions of
treatment with the antibodies and the Avastin.RTM. are indicated to
the left of the panels. The percentage of cells labelled with the
Annexin V-APC, corresponding to the percentage of cells having
entered into apoptosis, is indicated at the top-right of each
panel.
[0128] The cells cultured in the presence of the BZ1 control
antibody, with or without Avastin.RTM., exhibit respectively 12%
and 13% apoptosis. The apoptosis in the HT29-NRP-2 cells cultured
in the presence of the ITAC-B1 antibody is of the order of 51%, and
approximately 58% of the cells were pretreated with
Avastin.RTM..
[0129] These results clearly show that the neutralization of the
VEGF does not impair the ability of the ITAC-B1 antibody to induce
apoptosis, thereby confirming that the pro-apoptotic properties of
the ITAC-B1 antibody are VEGF-independent.
EXAMPLE 6
ITAC-B1 does not Influence Phosphorylation of the VEGFR1 Receptor
of the AKT Protein
[0130] The possible effect of the ITAC-B1 antibody on the degree of
phosphorylation of a VEGF receptor (VEGFR1), and also on the
phosphorylation of the AKT protein which is activated by means of
the VEGF receptors, was studied on HT29-NRP-2 and
Colo320.sup.siRNA-ctrl tumour cells.
[0131] The cells were cultured for 24 hours in RPMI medium+10% FCS
in the presence of the BZ1 control antibody at 20 .mu.g/ml, of
ITAC-B1 at 20 .mu.g/ml or of 5-FU at 50 .mu.g/ml. A "nontreated
cell" control was added ("medium" control). The cells were then
isolated and lysed, and the phosphorylation of VEGFR-1 and of AKT
was evaluated by Western blotting on the cell protein extracts,
using antibodies directed against nonphosphorylated VEGFR1
(anti-VEGFR1 rabbit polyclonal antibody) or phosphorylated VEGFR1
(anti-phospho-VEGFR1.sup.Tyr1213 rabbit polyclonal antibody,
R&D systems) or antibodies directed against nonphosphorylated
AKT (rabbit polyclonal antibody C67E7, Cell Signaling technology)
or phosphorylated AKT (anti-phospho-AKT.sup.Ser473 rabbit
polyclonal antibody DE-9, Cell Signaling technology). The results
are represented in FIGS. 16 and 17.
[0132] These results show that the phosphorylation status of VEGFR
and also the amount of AKT and its phosphorylation status are
similar, irrespective of whether or not the cells are treated with
ITAC-B1, demonstrating that the effects of this antibody are not
linked to the VEGF/VEGFR signalling pathway.
EXAMPLE 7
Search for any Interaction Between VEGF and the Neuropilin-2
Epitope Recognized by ITAC-B1
[0133] In order to demonstrate any competition between VEGFa and
ITAC-B1 for the recognition of neuropilin-2, HT29-NRP-2 tumour
cells expressing neuropilin-2 were preincubated with or without
VEGF (1000 ng/ml) for 15 minutes. These cells were then incubated
with the ITAC-B1 antibody or with a control isotype antibody (BZ1
antibody), and analysed by flow cytometry as described in Example 2
above.
[0134] The results are illustrated by FIG. 18. These results show
that the presence of VEGFa does not prevent the binding of ITAC-B1
to the tumour cells.
EXAMPLE 8
The ITAC-B1 and ITAC-B2 Antibodies have the Ability to Induce
Expression of the p53 Protein
[0135] After having shown that neuropilin-2 has the ability to
alter the expression of p53 in the HT29 line and to restore it in
the Colo320.sup.siRNA-NRP-2 line, the influence of the ITAC-B1
antibody on the expression of p53 in the lines expressing
neuropilin-2, such as HT29-NRP-2 and Colo320.sup.siRNA-ctrl was
studied.
[0136] The HT29, HT29-NRP-2, Colo320.sup.siRNA-ctrl tumour cells
and Colo320.sup.siRNA-NRP-2 were exposed to 20 ng/ml of ITAC-B1
antibody or of control antibody, and cultured for 48 hours. After
lysis of the cell lines, migration of the protein pellets obtained
on a 10% polyacrylamide gel (10 .mu.g of protein per well) and then
transfer onto a PVDF membrane, the membrane was incubated overnight
with the anti-p53 primary antibody (BD Biosciences, mouse
anti-human p53) diluted to 1/500. After washing in TBS/0.1%
Tween20, the membranes were incubated for 1 hour with an anti-mouse
IgG-HRP secondary antibody diluted to 1/6000. The results are
represented in FIG. 19.
[0137] These results show that the p53 protein is strongly
expressed in the HT29-ctrl and Colo320.sup.siRNA-NRP-2 lines which
do not express NRP-2, irrespective of whether or not the ITAC-B1
antibody is present in the medium. When the HT29-NRP-2 and
Colo320.sup.siRNA-ctrl lines which express NRP-2 are cultured alone
or in the presence of the control antibody, p53 is not detected,
while the presence of the ITAC-B1 antibody in the culture medium
partly restores the expression of p53. These results therefore show
that the treatment of cells expressing NRP-2 at their membrane
surface (HT29-NRP-2 and Colo320.sup.siRNA-ctrl) with ITAC-B1
results in restoration of the expression of p53 in the tumour
lines.
[0138] This experiment confirms that a negative correlation exists
between the presence of neuropilin-2 and of p53, and that ITAC-B1
has the original capacity of being able to modulate the level of
p53 expression.
EXAMPLE 7
Use of the ITAC-B1 Antibody to Potentiate the Effect of
Anti-Neoplastic Treatments In Vivo
[0139] HT29-NRP-2 tumour cells were injected subcutaneously into 20
immunodeficient mice, at a rate of 1.times.10.sup.6 cells per
mouse, in the right flank. 10 days after the injection, the tumours
measure approximately 5 mm.times.5 mm. Four groups of 3 mice having
comparable tumours were formed: each group received,
intraperitoneally, either PBS (control group A), or the ITAC-B1
antibody (group B), or 5-FU (group C), or 5-FU and the ITAC-B1
antibody (group D).
[0140] The chemotherapy treatment protocol is represented
schematically in FIG. 20.
[0141] In accordance with the protocol described above, group B was
inoculated with ITAC-B1 at D0 (12 mg/kg), D3 (6 mg/kg), D7 (12
mg/kg) and D10 (6 mg/kg). Group C was inoculated with 20 mg/kg of
5-FU from D0 to D4 and then with 100 mg/kg at D9. Group D was
inoculated with ITAC-B1 at D0 (12 mg/kg), D3 (6 mg/kg), D7 (12
mg/kg) and D10 (6 mg/kg) and with 20 mg/kg of 5-FU from D0 to D4
and 100 mg/kg of 5-FU at D9.
[0142] The tumours were measured twice a week, and the volume of
the tumours was calculated with the formula: V
(mm.sup.3)=d.sup.2.times.D/2. The results of these measurements are
shown in FIG. 21.
[0143] FIG. 21 represents the tumour volume as a function of time.
Group A (PBS control) is represented by (.diamond.), group B (mice
inoculated with the ITAC-B1 antibody) is represented by
(.box-solid.), group C (mice inoculated with 5-FU) is represented
by (.DELTA.), and group D (mice inoculated both with the ITAC-B1
antibody and with 5-FU) is represented by (x).
[0144] A reduction in tumour volume is observed starting from D14
in the mice inoculated with the ITAC-B1 antibody or with 5-FU. This
reduction is more marked during the combined 5-FU/ITAC-B1
treatment.
[0145] These results show that the ITAC-B1 antibody is capable of
slowing down tumour growth, in vivo. In addition, since the mice
treated with 5-FU combined with ITAC-B1 experience the greatest
slowing of tumour growth, compared with the mice treated with 5-FU
alone or ITAC-B1 alone, these results clearly show that the use of
the ITAC-B1 antibody potentiates the effectiveness of the
5-fluorouracil.
Sequence CWU 1
1
321349DNAMus
musculusCDS(1)..(348)V_region(1)..(294)misc_feature(1)..(75)FR1
1gaa gtt aag ctg cag gag tca ggg gca gag ctt gtg aag cca ggg gcc
48Glu Val Lys Leu Gln Glu Ser Gly Ala Glu Leu Val Lys Pro Gly Ala1
5 10 15tca gtc aag ttg tcc tgc aca gtt tct ggc ttc aac att aaa gac
acc 96Ser Val Lys Leu Ser Cys Thr Val Ser Gly Phe Asn Ile Lys Asp
Thr 20 25 30tat ata cac tgg gtg ata cag agg cct gaa cag ggc ctg gag
tgg ctt 144Tyr Ile His Trp Val Ile Gln Arg Pro Glu Gln Gly Leu Glu
Trp Leu 35 40 45gga agg att gat cct gcg aat ggt aat act aaa tat gac
ccg aag ttc 192Gly Arg Ile Asp Pro Ala Asn Gly Asn Thr Lys Tyr Asp
Pro Lys Phe 50 55 60cag ggc aag gcc act ata aca gca gac aca tcc tcc
aac aca gcc tac 240Gln Gly Lys Ala Thr Ile Thr Ala Asp Thr Ser Ser
Asn Thr Ala Tyr65 70 75 80ctg cag ctc agc agc ctg acc tct gag gac
act gcc gtc tat tac tgt 288Leu Gln Leu Ser Ser Leu Thr Ser Glu Asp
Thr Ala Val Tyr Tyr Cys 85 90 95gct aga tgg gcg gtt gta ggt gac tac
tgg ggc caa ggc acc act ctc 336Ala Arg Trp Ala Val Val Gly Asp Tyr
Trp Gly Gln Gly Thr Thr Leu 100 105 110aca gtc tcc tca g 349Thr Val
Ser Ser 1152116PRTMus musculus 2Glu Val Lys Leu Gln Glu Ser Gly Ala
Glu Leu Val Lys Pro Gly Ala1 5 10 15Ser Val Lys Leu Ser Cys Thr Val
Ser Gly Phe Asn Ile Lys Asp Thr 20 25 30Tyr Ile His Trp Val Ile Gln
Arg Pro Glu Gln Gly Leu Glu Trp Leu 35 40 45Gly Arg Ile Asp Pro Ala
Asn Gly Asn Thr Lys Tyr Asp Pro Lys Phe 50 55 60Gln Gly Lys Ala Thr
Ile Thr Ala Asp Thr Ser Ser Asn Thr Ala Tyr65 70 75 80Leu Gln Leu
Ser Ser Leu Thr Ser Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg
Trp Ala Val Val Gly Asp Tyr Trp Gly Gln Gly Thr Thr Leu 100 105
110Thr Val Ser Ser 1153318DNAMus
musculusV_region(1)..(283)misc_feature(1)..(77)FR1 3ga tat tgt gat
cac cca ctc tac aaa ttc ctg cat gta tca gca gga 47 Tyr Cys Asp His
Pro Leu Tyr Lys Phe Leu His Val Ser Ala Gly 1 5 10 15gac agg gtt
acc ata acc tgc aag gcc agt cag agt gtg agt gat gat 95Asp Arg Val
Thr Ile Thr Cys Lys Ala Ser Gln Ser Val Ser Asp Asp 20 25 30gtg gct
tgg tac caa cag aag cca ggg cag tct cct aaa ctg ctg ata 143Val Ala
Trp Tyr Gln Gln Lys Pro Gly Gln Ser Pro Lys Leu Leu Ile 35 40 45tac
tct gca tcc aat cgc tac act gga gtc cct gat cgc ttc act ggc 191Tyr
Ser Ala Ser Asn Arg Tyr Thr Gly Val Pro Asp Arg Phe Thr Gly 50 55
60agt gga tat ggg acg gat ttc act ttc acc atc agc act gtg cag cct
239Ser Gly Tyr Gly Thr Asp Phe Thr Phe Thr Ile Ser Thr Val Gln Pro
65 70 75gaa gac ctg gca gtt tat ttc tgt cag cag gat tat agc tct ccc
acg 287Glu Asp Leu Ala Val Tyr Phe Cys Gln Gln Asp Tyr Ser Ser Pro
Thr80 85 90 95ttc ggt tct ggg acc aag ctg gag ctg aaa c 318Phe Gly
Ser Gly Thr Lys Leu Glu Leu Lys 100 1054105PRTMus musculus 4Tyr Cys
Asp His Pro Leu Tyr Lys Phe Leu His Val Ser Ala Gly Asp1 5 10 15Arg
Val Thr Ile Thr Cys Lys Ala Ser Gln Ser Val Ser Asp Asp Val 20 25
30Ala Trp Tyr Gln Gln Lys Pro Gly Gln Ser Pro Lys Leu Leu Ile Tyr
35 40 45Ser Ala Ser Asn Arg Tyr Thr Gly Val Pro Asp Arg Phe Thr Gly
Ser 50 55 60Gly Tyr Gly Thr Asp Phe Thr Phe Thr Ile Ser Thr Val Gln
Pro Glu65 70 75 80Asp Leu Ala Val Tyr Phe Cys Gln Gln Asp Tyr Ser
Ser Pro Thr Phe 85 90 95Gly Ser Gly Thr Lys Leu Glu Leu Lys 100
1055358DNAMus
musculusCDS(1)..(357)V_region(1)..(295)misc_feature(1)..(75)FR1
5gag gtg cag ctg gag gag tca ggg gga ggc tta gtg aag cct gga ggg
48Glu Val Gln Leu Glu Glu Ser Gly Gly Gly Leu Val Lys Pro Gly Gly1
5 10 15tcc ctg aaa ctc tcc tgt gca gcc tct gga ttc act ttc agt gac
tat 96Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Asp
Tyr 20 25 30tac atg tat tgg gtt cgc cag act ccg gaa aag agg ctg gag
tgg gtc 144Tyr Met Tyr Trp Val Arg Gln Thr Pro Glu Lys Arg Leu Glu
Trp Val 35 40 45gca acc att agt gat ggt ggt agt tac acc tac tat cca
gac agt att 192Ala Thr Ile Ser Asp Gly Gly Ser Tyr Thr Tyr Tyr Pro
Asp Ser Ile 50 55 60aag ggc cga ttc acc atc tcc agg gac aat gcc agg
aac aac ctg tac 240Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Arg
Asn Asn Leu Tyr65 70 75 80ctt caa atg agc agt ctg aag tct gag gac
aca gcc atg tat tac tgt 288Leu Gln Met Ser Ser Leu Lys Ser Glu Asp
Thr Ala Met Tyr Tyr Cys 85 90 95gca aga ggt ggg ccc tat agg tcc tgg
ttt gct ttc tgg ggc caa ggg 336Ala Arg Gly Gly Pro Tyr Arg Ser Trp
Phe Ala Phe Trp Gly Gln Gly 100 105 110act ctg gtc act gtc tct gca
g 358Thr Leu Val Thr Val Ser Ala 1156119PRTMus musculus 6Glu Val
Gln Leu Glu Glu Ser Gly Gly Gly Leu Val Lys Pro Gly Gly1 5 10 15Ser
Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Asp Tyr 20 25
30Tyr Met Tyr Trp Val Arg Gln Thr Pro Glu Lys Arg Leu Glu Trp Val
35 40 45Ala Thr Ile Ser Asp Gly Gly Ser Tyr Thr Tyr Tyr Pro Asp Ser
Ile 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Arg Asn Asn
Leu Tyr65 70 75 80Leu Gln Met Ser Ser Leu Lys Ser Glu Asp Thr Ala
Met Tyr Tyr Cys 85 90 95Ala Arg Gly Gly Pro Tyr Arg Ser Trp Phe Ala
Phe Trp Gly Gln Gly 100 105 110Thr Leu Val Thr Val Ser Ala
1157337DNAMus
musculusCDS(1)..(336)V_region(1)..(302)misc_feature(1)..(78)FR1
7gat att gtg atc acc cag act cca ctc tcc ctg cct gtc agt ctt gga
48Asp Ile Val Ile Thr Gln Thr Pro Leu Ser Leu Pro Val Ser Leu Gly1
5 10 15gat caa gcc tcc atc tct tgc aga tct agt cag agc att gtg tat
agt 96Asp Gln Ala Ser Ile Ser Cys Arg Ser Ser Gln Ser Ile Val Tyr
Ser 20 25 30aat gga aac acc tat tta gaa tgg tac ctg cag aaa cca ggc
cag tct 144Asn Gly Asn Thr Tyr Leu Glu Trp Tyr Leu Gln Lys Pro Gly
Gln Ser 35 40 45cca aag ctc ctg atc tac aaa gtt tcc aac cga ttt tct
ggg gtc cca 192Pro Lys Leu Leu Ile Tyr Lys Val Ser Asn Arg Phe Ser
Gly Val Pro 50 55 60gac agg ttc agt ggc agt gga tca ggg aca gat ttc
aca ctc aag atc 240Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe
Thr Leu Lys Ile65 70 75 80agc aga gtg gag gct gag gat ctg gga gtt
tat tac tgc ttt caa ggt 288Ser Arg Val Glu Ala Glu Asp Leu Gly Val
Tyr Tyr Cys Phe Gln Gly 85 90 95tca cat gtt cct ccg acg ttc ggt gga
ggc acc aag ctg gaa atc aaa c 337Ser His Val Pro Pro Thr Phe Gly
Gly Gly Thr Lys Leu Glu Ile Lys 100 105 1108112PRTMus musculus 8Asp
Ile Val Ile Thr Gln Thr Pro Leu Ser Leu Pro Val Ser Leu Gly1 5 10
15Asp Gln Ala Ser Ile Ser Cys Arg Ser Ser Gln Ser Ile Val Tyr Ser
20 25 30Asn Gly Asn Thr Tyr Leu Glu Trp Tyr Leu Gln Lys Pro Gly Gln
Ser 35 40 45Pro Lys Leu Leu Ile Tyr Lys Val Ser Asn Arg Phe Ser Gly
Val Pro 50 55 60Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr
Leu Lys Ile65 70 75 80Ser Arg Val Glu Ala Glu Asp Leu Gly Val Tyr
Tyr Cys Phe Gln Gly 85 90 95Ser His Val Pro Pro Thr Phe Gly Gly Gly
Thr Lys Leu Glu Ile Lys 100 105 11098PRTMus musculus 9Gly Phe Asn
Ile Lys Asp Thr Tyr1 5108PRTMus musculus 10Ile Asp Pro Ala Asn Gly
Asn Thr1 5119PRTMus musculus 11Ala Arg Trp Ala Val Val Gly Asp Tyr1
5126PRTMus musculus 12Gln Ser Val Ser Asp Asp1 5133PRTMus musculus
13Ser Ala Ser1148PRTMus musculus 14Gln Gln Asp Tyr Ser Ser Pro Thr1
5158PRTMus musculus 15Gly Phe Thr Phe Ser Asp Tyr Tyr1 5168PRTMus
musculus 16Ile Ser Asp Gly Gly Ser Tyr Thr1 51712PRTMus musculus
17Ala Arg Gly Gly Pro Tyr Arg Ser Trp Phe Ala Phe1 5 101811PRTMus
musculus 18Gln Ser Ile Val Tyr Ser Asn Gly Asn Thr Tyr1 5
10193PRTMus musculus 19Lys Val Ser1209PRTMus musculus 20Phe Gln Gly
Ser His Val Pro Pro Thr1 52123DNAArtificial SequenceSynthetic PCR
PRIMER 21gargttaagc tgsaggagtc agg 232227DNAArtificial
SequenceSynthetic PCR PRIMER 22atagacagat gggggtgtcg ttttggc
272323DNAArtificial SequenceSynthetic PCR PRIMER 23gaggtgcagc
tggaggagtc agg 232427DNAArtificial SequenceSynthetic PCR PRIMER
24atagacagat gggggtgtcg ttttggc 272524DNAArtificial
SequenceSynthetic PCR PRIMER 25gatattgtga tsacmcardc taca
242622DNAArtificial SequenceSynthetic PCR PRIMER 26ggatacagtt
ggtgcagcat ta 222724DNAArtificial SequenceSynthetic PCR PRIMER
27gatattgtgm tsacccagac tcca 242822DNAArtificial SequenceSynthetic
PCR PRIMER 28ggatacagtt ggtgcagcat ta 222923DNAHomo sapiens
29aaaggctgga agtcagcact aat 233023DNAHomo sapiens 30aaaaattagt
gctgacttcc agc 233122RNAArtificialSynthetic siRNA 31ggcuggaagu
cagcacuaau uu 223222RNAArtificialSynthetic siRNA 32auuagugcug
acuuccagcc uu 22
* * * * *